ES2534318B1 - Derivados de cromeno sustituidos por alcóxido como inhibidores de la interacción TCR-Nck - Google Patents
Derivados de cromeno sustituidos por alcóxido como inhibidores de la interacción TCR-Nck Download PDFInfo
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- ES2534318B1 ES2534318B1 ES201331542A ES201331542A ES2534318B1 ES 2534318 B1 ES2534318 B1 ES 2534318B1 ES 201331542 A ES201331542 A ES 201331542A ES 201331542 A ES201331542 A ES 201331542A ES 2534318 B1 ES2534318 B1 ES 2534318B1
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- ethyl acetate
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- 150000004703 alkoxides Chemical group 0.000 title abstract 2
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- 239000003112 inhibitor Substances 0.000 title abstract 2
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- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 87
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/74—Benzo[b]pyrans, hydrogenated in the carbocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
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- Animal Behavior & Ethology (AREA)
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- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrane Compounds (AREA)
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES201331542A ES2534318B1 (es) | 2013-10-18 | 2013-10-18 | Derivados de cromeno sustituidos por alcóxido como inhibidores de la interacción TCR-Nck |
CN201480057192.8A CN105658634B (zh) | 2013-10-18 | 2014-10-20 | 作为TCR-Nck相互作用的抑制剂的被醇盐取代的色烯衍生物 |
EP14809703.3A EP3059232B1 (en) | 2013-10-18 | 2014-10-20 | Chromene derivatives substituted by alkoxide as inhibitors of the tcr-nck interaction |
RU2016118037A RU2658910C2 (ru) | 2013-10-18 | 2014-10-20 | Производные хромена, замещённые посредством алкоксида, в качестве ингибиторов взаимодействия tcr-nck |
AU2014335859A AU2014335859B2 (en) | 2013-10-18 | 2014-10-20 | Chromene derivatives substituted by alkoxide as inhibitors of the TCR-Nck interaction |
JP2016522733A JP6505095B2 (ja) | 2013-10-18 | 2014-10-20 | Tcr−nck相互作用の阻害剤としての、アルコキシドによって置換されたクロメン誘導体 |
PCT/IB2014/002171 WO2015056085A1 (es) | 2013-10-18 | 2014-10-20 | Derivados de cromeno sustituidos por alcóxido como inhibidores de la interacción tcr-nck |
ES14809703T ES2719115T3 (es) | 2013-10-18 | 2014-10-20 | Derivados de cromeno sustituidos por alcóxido como inhibidores de la interacción TCR-Nck |
CA2925846A CA2925846C (en) | 2013-10-18 | 2014-10-20 | Chromene derivatives substituted by alkoxide as inhibitors of the tcr-nck interaction |
US15/029,042 US10131647B2 (en) | 2013-10-18 | 2014-10-20 | Chromene derivatives substituted by alkoxide as inhibitors of the TCR-Nck interaction |
HK16114566A HK1226388A1 (zh) | 2013-10-18 | 2016-12-22 | 作為tcr-nck相互作用的抑制劑的被醇鹽取代的色烯衍生物 |
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ES201331542A ES2534318B1 (es) | 2013-10-18 | 2013-10-18 | Derivados de cromeno sustituidos por alcóxido como inhibidores de la interacción TCR-Nck |
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ES14809703T Active ES2719115T3 (es) | 2013-10-18 | 2014-10-20 | Derivados de cromeno sustituidos por alcóxido como inhibidores de la interacción TCR-Nck |
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EP (1) | EP3059232B1 (zh) |
JP (1) | JP6505095B2 (zh) |
CN (1) | CN105658634B (zh) |
AU (1) | AU2014335859B2 (zh) |
CA (1) | CA2925846C (zh) |
ES (2) | ES2534318B1 (zh) |
HK (1) | HK1226388A1 (zh) |
RU (1) | RU2658910C2 (zh) |
WO (1) | WO2015056085A1 (zh) |
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ES2534336B1 (es) * | 2013-10-18 | 2016-01-28 | Artax Biopharma Inc. | Derivados de cromeno como inhibidores de la interacción TCR-Nck |
EA037785B1 (ru) | 2016-04-12 | 2021-05-21 | Джапан Тобакко Инк. | Ароматический ингалятор |
SG11202008067QA (en) * | 2018-02-27 | 2020-09-29 | Artax Biopharma Inc | Chromene derivatives as inhibitors of tcr-nck interaction |
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UA62993C2 (en) * | 1997-12-19 | 2004-01-15 | Bayer Ag | CHROMAN DERIVATIVES SUBSTITUTED ON CARBOXYLIC GROUP USED AS AGONISTS OF b-3-ADRENORECEPTOR |
DE19858341A1 (de) * | 1998-12-17 | 2000-06-21 | Merck Patent Gmbh | Chromanderivate |
EP1230232B1 (en) | 1999-11-05 | 2004-02-25 | Cytovia, Inc. | Substituted 4h-chromene and analogs as activators of caspases and inducers of apoptosis and the use thereof |
AU2001278980A1 (en) | 2000-07-21 | 2002-02-05 | Chugai Seiyaku Kabushiki Kaisha | Coumarin derivatives useful as tnfalpha inhibitors |
EP1392283A4 (en) | 2001-05-16 | 2004-10-20 | Cytovia Inc | COUMARINS AND SUBSTITUTED QUINOLINES USED AS CASPASE ACTIVATORS |
WO2003062272A1 (es) | 2002-01-24 | 2003-07-31 | Consejo Superior De Investigaciones Científicas | Nueva estrategia moduladora de la activacion de los linfocitos t basada en la regulación de la interaccion cd3e- nck. |
WO2003096982A2 (en) | 2002-05-16 | 2003-11-27 | Cytovia, Inc. | Substituted 4h-chromenes, 2h-chromenes, chromans and analogs as activators of caspases and inducers of apoptosis and the use thereof |
GB0607389D0 (en) | 2006-04-12 | 2006-05-24 | Novartis Ag | Organic compounds |
ES2331451B1 (es) | 2008-06-30 | 2010-10-21 | Consejo Superior De Investigaciones Cientificas (Csic) | Inmunosupresor basado en la interrupcion de la interaccion tcr-nck. |
JP2011528359A (ja) | 2008-07-16 | 2011-11-17 | ブリストル−マイヤーズ スクイブ カンパニー | ケモカイン受容体活性のクロメンモジュレーター |
RU2490266C2 (ru) * | 2008-12-05 | 2013-08-20 | Астеллас Фарма Инк. | Соединение 2н-хромена и его производное |
ES2379242B1 (es) | 2010-09-28 | 2013-03-04 | Consejo Superior De Investigaciones Científicas (Csic) | Derivados de cromeno. |
ES2534336B1 (es) | 2013-10-18 | 2016-01-28 | Artax Biopharma Inc. | Derivados de cromeno como inhibidores de la interacción TCR-Nck |
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2013
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2014
- 2014-10-20 JP JP2016522733A patent/JP6505095B2/ja active Active
- 2014-10-20 WO PCT/IB2014/002171 patent/WO2015056085A1/es active Application Filing
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- 2014-10-20 CA CA2925846A patent/CA2925846C/en active Active
- 2014-10-20 CN CN201480057192.8A patent/CN105658634B/zh active Active
- 2014-10-20 RU RU2016118037A patent/RU2658910C2/ru active
- 2014-10-20 US US15/029,042 patent/US10131647B2/en active Active
- 2014-10-20 AU AU2014335859A patent/AU2014335859B2/en active Active
- 2014-10-20 EP EP14809703.3A patent/EP3059232B1/en active Active
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Also Published As
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US10131647B2 (en) | 2018-11-20 |
AU2014335859B2 (en) | 2018-11-01 |
ES2534318A1 (es) | 2015-04-21 |
CA2925846A1 (en) | 2015-04-23 |
CN105658634B (zh) | 2019-01-22 |
CA2925846C (en) | 2019-02-19 |
HK1226388A1 (zh) | 2017-09-29 |
US20160244423A1 (en) | 2016-08-25 |
JP6505095B2 (ja) | 2019-04-24 |
CN105658634A (zh) | 2016-06-08 |
WO2015056085A1 (es) | 2015-04-23 |
ES2719115T3 (es) | 2019-07-08 |
JP2017506209A (ja) | 2017-03-02 |
RU2016118037A (ru) | 2017-11-23 |
AU2014335859A1 (en) | 2016-05-05 |
EP3059232A1 (en) | 2016-08-24 |
EP3059232B1 (en) | 2019-01-09 |
RU2658910C2 (ru) | 2018-06-26 |
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